Reversed papilledema in an MPS VI patient with galsulfase (Naglazyme(®)) therapy

MPS VI (mucopolysaccharidosis VI, known as Maroteaux–Lamy syndrome) is a multi-systemic inherited disease, resulting from a deficiency of N-acetylgalactosamine-4-sulfatase, causing accumulation of the glycosaminoglycan (GAG) dermatan sulfate in all tissues. It is one of almost 50 lysosomal storage d...

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Detalles Bibliográficos
Autores principales: Koseoglu, Selim T., Harmatz, Paul, Turbeville, Sean, Nicely, Helen
Formato: Texto
Lenguaje:English
Publicado: Springer Netherlands 2008
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2714452/
https://www.ncbi.nlm.nih.gov/pubmed/18418554
http://dx.doi.org/10.1007/s10792-008-9213-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2714452/
https://www.ncbi.nlm.nih.gov/pubmed/18418554
http://dx.doi.org/10.1007/s10792-008-9213-7

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